Canonical Allele Identifier: CA1926173623

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965324_87965325delinsCA , CM000672.2:g.87965324_87965325delinsCA	GRCh38
NC_000010.10:g.89725081_89725082delinsCA , CM000672.1:g.89725081_89725082delinsCA	GRCh37
NC_000010.9:g.89715061_89715062delinsCA	NCBI36
NG_007466.2:g.106886_106887delinsCA , LRG_311:g.106886_106887delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1157_1158delinsCA	ENSP00000514759.2:p.Ser386=
ENST00000710265.1:c.*93_*94delinsCA	ENSP00000518161.1:n.*93_*94delinsCA
ENST00000688158.2:n.1799_1800delinsCA
ENST00000688922.2:c.*894_*895delinsCA	ENSP00000508742.2:n.*894_*895delinsCA
ENST00000700021.1:c.1019_1020delinsCA	ENSP00000514757.1:p.Ser340=
ENST00000700022.1:c.*403_*404delinsCA	ENSP00000514758.1:n.*403_*404delinsCA
ENST00000700023.1:n.2222_2223delinsCA
ENST00000700024.1:n.2456_2457delinsCA
ENST00000706954.1:c.1064_1065delinsCA	ENSP00000516674.1:p.Ser355=
ENST00000706955.1:c.*1099_*1100delinsCA	ENSP00000516675.1:n.*1099_*1100delinsCA
ENST00000686459.1:c.*650_*651delinsCA	ENSP00000508909.1:n.*650_*651delinsCA
ENST00000688158.1:c.*1175_*1176delinsCA	ENSP00000509254.1:n.*1175_*1176delinsCA
ENST00000688308.1:c.1064_1065delinsCA	ENSP00000508752.1:p.Ser355=
ENST00000688922.1:c.985_986delinsCA
ENST00000693560.1:c.1583_1584delinsCA	ENSP00000509861.1:p.Ser528=
ENST00000371953.8:c.1064_1065delinsCA MANE Select	ENSP00000361021.3:p.Ser355=
ENST00000371953.7:c.1064_1065delinsCA	ENSP00000361021.3:p.Ser355=
NM_000314.5:c.1064_1065delinsCA	NP_000305.3:p.Ser355=
NM_000314.6:c.1064_1065delinsCA	NP_000305.3:p.Ser355=
NM_001304717.2:c.1583_1584delinsCA	NP_001291646.2:p.Ser528=
NM_001304718.1:c.473_474delinsCA	NP_001291647.1:p.Ser158=
XM_006717926.2:c.1019_1020delinsCA	XP_006717989.1:p.Ser340=
XM_011539982.1:c.968_969delinsCA	XP_011538284.1:p.Ser323=
XR_945791.1:n.1634_1635delinsCA
NM_000314.7:c.1064_1065delinsCA	NP_000305.3:p.Ser355=
NM_001304717.5:c.1583_1584delinsCA	NP_001291646.4:p.Ser528=
NM_001304718.2:c.473_474delinsCA	NP_001291647.1:p.Ser158=
NM_000314.8:c.1064_1065delinsCA MANE Select	NP_000305.3:p.Ser355=